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rs17128077

From SNPedia

Orientationplus
Stabilizedplus
Make rs17128077(C;C)
Make rs17128077(C;T)
Make rs17128077(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position54919316
is asnp
is mentioned by
dbSNPrs17128077
dbSNP (old)rs17128077
ClinGenrs17128077
ebirs17128077
HLIrs17128077
Exacrs17128077
Gnomadrs17128077
Varsomers17128077
Maprs17128077
PheGenIrs17128077
Biobankrs17128077
1000 genomesrs17128077
hgdprs17128077
ensemblrs17128077
gopubmedrs17128077
geneviewrs17128077
scholarrs17128077
googlers17128077
pharmgkbrs17128077
gwascentralrs17128077
openSNPrs17128077
23andMers17128077
23andMe allrs17128077
SNP Nexus

SNPshotrs17128077
SNPdbers17128077
MSV3drs17128077
GWAS Ctlgrs17128077
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 26215833OA-icon.png] Nucleotide Variants of the BH4 Biosynthesis Pathway Gene GCH1 and the Risk of Orofacial Clefts